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FDA 510(k)

SUTURE REMOVAL PAK

K-Number: K801746 · 1980-08-20

ApplicantDevco Medical Industries, Inc.
Decision Date1980-08-20
Product CodeFZT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUTURE REMOVAL PAK is the device name listed in this FDA 510(k) record. The listed applicant is Devco Medical Industries, Inc.. It received FDA 510(k) clearance on 1980-08-20 under 510(k) number K801746. The device is classified under product code FZT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUTURE REMOVAL PAK?

SUTURE REMOVAL PAK is a medical device that received FDA 510(k) clearance on 1980-08-20. The listed applicant is Devco Medical Industries, Inc.. The 510(k) number is K801746.

When did SUTURE REMOVAL PAK receive FDA 510(k) clearance?

SUTURE REMOVAL PAK received FDA 510(k) clearance on 1980-08-20, under 510(k) number K801746.

Who is the listed applicant for SUTURE REMOVAL PAK?

The FDA 510(k) record lists Devco Medical Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUTURE REMOVAL PAK?

The FDA product code for SUTURE REMOVAL PAK is FZT.

Related Clinical Trials

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Related Devices (Code: FZT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K112400SMARTSHEARSNuscience Consulting and Management Group, LLCK890818AUTO SUTURE DISPOSABLE SURGICAL TROCAR*United States Surgical, A Division of Tyco HealthcK872990MICRINS SURGICAL SCISSORMicrins Surgical, Inc.K841741SINGLE HAIR TRANSPLANT GRAFTParis Products, Inc.K841247SPC DISPOSABLE CUTTERSurgical Products Corp.K822448SCISSORS, VARIOUSJ. Sklar Mfg. Co., Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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